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Detection of Differentially Expressed MicroRNAs in Rheumatic Heart Disease: miR-1183 and miR-1299 as Potential Diagnostic Biomarkers

This study compared microRNA (miRNA) expression profiles between rheumatic heart disease (RHD) patients and healthy controls to investigate their differential expression and help elucidate their mechanisms of action. Microarray analysis was used to measure miRNA expression, and a total of 133 miRNAs...

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Detalles Bibliográficos
Autores principales: Li, Ni, Lian, Jiangfang, Zhao, Sheng, Zheng, Dawei, Yang, Xi, Huang, Xiaoyan, Shi, Xinbao, Sun, Lebo, Zhou, Qingyun, Shi, Huoshun, Xu, Guodong, Incoom, Enchill KoJo, Zhou, Jianqing, Shao, Guofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619814/
https://www.ncbi.nlm.nih.gov/pubmed/26539505
http://dx.doi.org/10.1155/2015/524519
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author Li, Ni
Lian, Jiangfang
Zhao, Sheng
Zheng, Dawei
Yang, Xi
Huang, Xiaoyan
Shi, Xinbao
Sun, Lebo
Zhou, Qingyun
Shi, Huoshun
Xu, Guodong
Incoom, Enchill KoJo
Zhou, Jianqing
Shao, Guofeng
author_facet Li, Ni
Lian, Jiangfang
Zhao, Sheng
Zheng, Dawei
Yang, Xi
Huang, Xiaoyan
Shi, Xinbao
Sun, Lebo
Zhou, Qingyun
Shi, Huoshun
Xu, Guodong
Incoom, Enchill KoJo
Zhou, Jianqing
Shao, Guofeng
author_sort Li, Ni
collection PubMed
description This study compared microRNA (miRNA) expression profiles between rheumatic heart disease (RHD) patients and healthy controls to investigate their differential expression and help elucidate their mechanisms of action. Microarray analysis was used to measure miRNA expression, and a total of 133 miRNAs were shown to be significantly upregulated in RHD patients compared with controls, including miR-1183 and miR-1299. A total of 137 miRNAs, including miR-4423-3p and miR-218-1-3p, were significantly downregulated in RHD patients. Quantitative real-time-PCR confirmed microarray findings for miR-1183 and miR-1299 in both tissue and plasma. Bioinformatic predictions were also made of differentially expressed miRNAs as biomarkers in RHD by databases and GO/pathway analysis. Furthermore, we investigated miR-1183 and miR-1299 expression in RHD patients with secondary pulmonary hypertension (PAH). Our findings identified an important role for miR-1299 as a direct regulator of RHD, while the observed difference in expression of miR-1183 between RHD-PAH patients with high or low pulmonary artery pressure suggests that miR-1183 overexpression may reflect pulmonary artery remodeling. miR-1183 and miR-1299 appear to play distinct roles in RHD pathogenesis accompanied by secondary PAH and could be used as potential biological markers for disease development.
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spelling pubmed-46198142015-11-04 Detection of Differentially Expressed MicroRNAs in Rheumatic Heart Disease: miR-1183 and miR-1299 as Potential Diagnostic Biomarkers Li, Ni Lian, Jiangfang Zhao, Sheng Zheng, Dawei Yang, Xi Huang, Xiaoyan Shi, Xinbao Sun, Lebo Zhou, Qingyun Shi, Huoshun Xu, Guodong Incoom, Enchill KoJo Zhou, Jianqing Shao, Guofeng Biomed Res Int Research Article This study compared microRNA (miRNA) expression profiles between rheumatic heart disease (RHD) patients and healthy controls to investigate their differential expression and help elucidate their mechanisms of action. Microarray analysis was used to measure miRNA expression, and a total of 133 miRNAs were shown to be significantly upregulated in RHD patients compared with controls, including miR-1183 and miR-1299. A total of 137 miRNAs, including miR-4423-3p and miR-218-1-3p, were significantly downregulated in RHD patients. Quantitative real-time-PCR confirmed microarray findings for miR-1183 and miR-1299 in both tissue and plasma. Bioinformatic predictions were also made of differentially expressed miRNAs as biomarkers in RHD by databases and GO/pathway analysis. Furthermore, we investigated miR-1183 and miR-1299 expression in RHD patients with secondary pulmonary hypertension (PAH). Our findings identified an important role for miR-1299 as a direct regulator of RHD, while the observed difference in expression of miR-1183 between RHD-PAH patients with high or low pulmonary artery pressure suggests that miR-1183 overexpression may reflect pulmonary artery remodeling. miR-1183 and miR-1299 appear to play distinct roles in RHD pathogenesis accompanied by secondary PAH and could be used as potential biological markers for disease development. Hindawi Publishing Corporation 2015 2015-10-11 /pmc/articles/PMC4619814/ /pubmed/26539505 http://dx.doi.org/10.1155/2015/524519 Text en Copyright © 2015 Ni Li et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Ni
Lian, Jiangfang
Zhao, Sheng
Zheng, Dawei
Yang, Xi
Huang, Xiaoyan
Shi, Xinbao
Sun, Lebo
Zhou, Qingyun
Shi, Huoshun
Xu, Guodong
Incoom, Enchill KoJo
Zhou, Jianqing
Shao, Guofeng
Detection of Differentially Expressed MicroRNAs in Rheumatic Heart Disease: miR-1183 and miR-1299 as Potential Diagnostic Biomarkers
title Detection of Differentially Expressed MicroRNAs in Rheumatic Heart Disease: miR-1183 and miR-1299 as Potential Diagnostic Biomarkers
title_full Detection of Differentially Expressed MicroRNAs in Rheumatic Heart Disease: miR-1183 and miR-1299 as Potential Diagnostic Biomarkers
title_fullStr Detection of Differentially Expressed MicroRNAs in Rheumatic Heart Disease: miR-1183 and miR-1299 as Potential Diagnostic Biomarkers
title_full_unstemmed Detection of Differentially Expressed MicroRNAs in Rheumatic Heart Disease: miR-1183 and miR-1299 as Potential Diagnostic Biomarkers
title_short Detection of Differentially Expressed MicroRNAs in Rheumatic Heart Disease: miR-1183 and miR-1299 as Potential Diagnostic Biomarkers
title_sort detection of differentially expressed micrornas in rheumatic heart disease: mir-1183 and mir-1299 as potential diagnostic biomarkers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619814/
https://www.ncbi.nlm.nih.gov/pubmed/26539505
http://dx.doi.org/10.1155/2015/524519
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